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Floodplain soils are subject to quasi-periodic flood disturbances. This flooding serves to enrich floodplain soils, increasing their fertility and often making them ideal locations for agriculture. However, what is less well understood is how the frequency of flooding impacts on soil fertility and the diversity of soil character. This study investigates how flood frequency influences the heterogeneity (assessed using 26 physical and geochemical soil properties) of floodplain soils in a semi-arid floodplain wetland system in New South Wales, Australia. The study includes an investigation of soil properties across four flood frequency (or disturbance frequency) categories ranging from frequent through to infrequent flood disturbance. Thirty samples were collected from each zone and the physical and geochemical soil data were analyzed using a suite of univariate and multivariate statistical tests. The results show that sites subject to an intermediate level of flood disturbance have a greater level of diversity in soil properties than those sites subject to frequent flood disturbances. These results reflect those of the Intermediate Disturbance Hypothesis, an ecological theory that posits the highest biological diversity will also be found in intermediately disturbed environments and suggests that there might be physical habitat drivers of biological diversity in intermediately disturbed floodplains. [ABSTRACT FROM AUTHOR]

Diverse neurons in the parabrachial nucleus (PB) communicate with widespread brain regions. Despite evidence linking them to a variety of homeostatic functions, it remains difficult to determine which PB neurons influence which functions because their subpopulations intermingle extensively. An improved framework for identifying these intermingled subpopulations would help advance our understanding of neural circuit functions linked to this region. Here, we present the foundation of a developmental‐genetic ontology that classifies PB neurons based on their intrinsic, molecular features. By combining transcription factor labeling with Cre fate‐mapping, we find that the PB is a blend of two, developmentally distinct macropopulations of glutamatergic neurons. Neurons in the first macropopulation express Lmx1b (and, to a lesser extent, Lmx1a) and are mutually exclusive with those in a second macropopulation, which derive from precursors expressing Atoh1. This second, Atoh1‐derived macropopulation includes many Foxp2‐expressing neurons, but Foxp2 also identifies a subset of Lmx1b‐expressing neurons in the Kölliker–Fuse nucleus (KF) and a population of GABAergic neurons ventrolateral to the PB ("caudal KF"). Immediately ventral to the PB, Phox2b‐expressing glutamatergic neurons (some coexpressing Lmx1b) occupy the KF, supratrigeminal nucleus, and reticular formation. We show that this molecular framework organizes subsidiary patterns of adult gene expression (including Satb2, Calca, Grp, and Pdyn) and predicts output projections to the amygdala (Lmx1b), hypothalamus (Atoh1), and hindbrain (Phox2b/Lmx1b). Using this molecular ontology to organize, interpret, and communicate PB‐related information could accelerate the translation of experimental findings from animal models to human patients. [ABSTRACT FROM AUTHOR]

The parabrachial nucleus (PB) is composed of glutamatergic neurons at the midbrain–hindbrain junction. These neurons form many subpopulations, one of which expresses Calca, which encodes the neuropeptide calcitonin gene‐related peptide (CGRP). This Calca‐expressing subpopulation has been implicated in a variety of homeostatic functions, but the overall distribution of Calca‐expressing neurons in this region remains unclear. Also, while previous studies in rats and mice have identified output projections from CGRP‐immunoreactive or Calca‐expressing neurons, we lack a comprehensive understanding of their efferent projections. We began by identifying neurons with Calca mRNA and CGRP immunoreactivity in and around the PB, including populations in the locus coeruleus and motor trigeminal nucleus. Calca‐expressing neurons in the PB prominently express the mu opioid receptor (Oprm1) and are distinct from neighboring neurons that express Foxp2 and Pdyn. Next, we used Cre‐dependent anterograde tracing with synaptophysin‐mCherry to map the efferent projections of these neurons. Calca‐expressing PB neurons heavily target subregions of the amygdala, bed nucleus of the stria terminalis, basal forebrain, thalamic intralaminar and ventral posterior parvicellular nuclei, and hindbrain, in different patterns depending on the injection site location within the PB region. Retrograde axonal tracing revealed that the previously unreported hindbrain projections arise from a rostral‐ventral subset of CGRP/Calca neurons. Finally, we show that these efferent projections of Calca‐expressing neurons are distinct from those of neighboring PB neurons that express Pdyn. This information provides a detailed neuroanatomical framework for interpreting experimental work involving CGRP/Calca‐expressing neurons and opioid action in the PB region. [ABSTRACT FROM AUTHOR]